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1.
J Autism Dev Disord ; 51(12): 4354-4369, 2021 Dec.
Article in English | MEDLINE | ID: mdl-33866461

ABSTRACT

Commemorating the 40 th anniversary of the Diagnostic and Statistical Manual (DSM) III, the purpose of this commentary is to describe school-based and school-relevant interventions and instructional approaches for children and youth with autism that have been developed and employed during that time period. The commentary begins with a brief description of foundational research that provides an historical context. Research themes shaped by science, ethics, social policy, and the changes in the DSM provide an organization for describing the evolution of intervention and instructional practices over the four previous decades. The commentary concludes with a discussion of school-contextual variables that influence implementation and the promise of the "iSciences" for closing the research to practice gap in the future.


Subject(s)
Autism Spectrum Disorder , Autistic Disorder , Adolescent , Autism Spectrum Disorder/diagnosis , Autism Spectrum Disorder/therapy , Autistic Disorder/therapy , Child , Humans , Schools
2.
Autism ; 24(3): 707-717, 2020 04.
Article in English | MEDLINE | ID: mdl-31747775

ABSTRACT

The purpose of the study was to examine the quality of high school programs for students with autism spectrum disorder in the United States. The Autism Program Environment Rating Scale-Middle/High School was used to rate the quality of programs for students with autism spectrum disorder in 60 high schools located in three geographic locations in the United States (CA, NC, and WI). Findings indicated that the total quality rating across schools was slightly above the adequate criterion. Higher quality ratings occurred for program environment, learning climate, family participation, and teaming domains. However, quality ratings for intervention domains related to the characteristics of autism spectrum disorder (e.g. communication, social, independence, functional behavior, and transition) were below the adequate quality rating level. Also, quality ratings for transition were significantly higher for modified (primarily self-contained) programs than standard diploma (primarily served in general education) programs. School urbanicity was a significant predictor of program quality, with suburban schools having higher quality ratings than urban or rural schools, controlling for race, school enrollment size, and Title 1 eligibility status. Implications for working with teachers and school teams that support high school students with autism spectrum disorder should include a targeted focus on transition programming that includes a breadth of work-based learning experiences and activities that support social-communication domains.


Subject(s)
Autism Spectrum Disorder , Quality of Life , Schools/organization & administration , Schools/standards , Students , Adolescent , Autism Spectrum Disorder/psychology , Child , Communication , Female , Humans , Male , Social Interaction , Students/psychology , Students/statistics & numerical data , Young Adult
3.
Intellect Dev Disabil ; 47(1): 31-43, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19170417

ABSTRACT

The transition from high school to adulthood is a critical life stage that entails many changes, especially for youth with severe intellectual disability. The transition period may be especially stressful for the families of these young adults, who often experience a sudden change, or decrease, in services. However, little research has examined what constitutes a successful transition for the families of these individuals. The present study examined parent perspectives of transition for 128 young adults with severe intellectual disability, specifically, parent satisfaction with transition. Results suggested that transition satisfaction is related to young adult, family, and environmental characteristics, with environmental characteristics being the strongest predictors of transition satisfaction. Furthermore, transition satisfaction is related to multiple measures of family well being, indicating the tremendous need for considering the broader family system when planning for a young adult's transition. Implications and directions for future research are discussed.


Subject(s)
Family/psychology , Intellectual Disability , Parent-Child Relations , Patient Satisfaction , Quality of Life/psychology , Female , Humans , Male , Middle Aged , Severity of Illness Index , Young Adult
4.
Ment Retard ; 41(4): 250-62, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12862511

ABSTRACT

The quality of life of 188 young adults with moderate or severe mental retardation was examined. Schalock and Keith's (1993) Quality of Life Questionnaire (QOL-Q) was used as the primary outcome measure. Young adults who had exited high school had significantly higher overall quality of life scores than did those who were still attending school. Individuals who had jobs in the community also had significantly higher levels of quality of life. Although young adult adaptive functioning was the single largest indicator of the QOL-Q index total score and three of the four subscales, it was not related to scores on the Satisfaction subscale. Here, family- and environment-related variables played a greater role. Implications and directions for future research are discussed.


Subject(s)
Intellectual Disability/psychology , Quality of Life , Adult , California , Educational Status , Employment, Supported , Female , Humans , Intellectual Disability/classification , Male , Severity of Illness Index , Sickness Impact Profile , Surveys and Questionnaires
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